loading...| Preferred Name |
Antithrombin III Deficiency |
|
| Synonyms |
Antithrombin III Deficiency |
|
| Definitions |
A rare disorder characterized by the presence of low levels of antithrombin III which prohibits the formation of blood clots. It may be inherited, usually in an autosomal dominant pattern, or acquired. It may lead to venous thrombosis and pulmonary embolism. |
|
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C98815 |
|
| ALT_DEFINITION |
A rare disorder characterized by the presence of low levels of antithrombin III which prohibits the formation of blood clots. It may be inherited, usually in an autosomal dominant pattern, or acquired. It may lead to venous thrombosis and pulmonary embolism. |
|
| code |
C98815 |
|
| Concept_In_Subset |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C90259 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C192842 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C165258 |
|
| Contributing_Source |
Cellosaurus NICHD |
|
| DEFINITION |
A rare disorder characterized by the presence of low levels of antithrombin III which prohibits the formation of blood clots. It may be inherited, usually in an autosomal dominant pattern, or acquired. It may lead to venous thrombosis and pulmonary embolism. |
|
| FULL_SYN |
Antithrombin III Deficiency |
|
| label |
Antithrombin III Deficiency |
|
| Preferred_Name |
Antithrombin III Deficiency |
|
| prefixIRI |
Thesaurus:C98815 |
|
| Related_To_Genetic_Biomarker | ||
| Semantic_Type |
Disease or Syndrome |
|
| UMLS_CUI |
C3807759 |
|
| subClassOf |